Like A A, Weringer E J, Holdash A, McGill P, Atkinson D, Rossini A A
J Immunol. 1985 Mar;134(3):1583-7.
Adoptive transfer of diabetes was accomplished by the injection of Con A-activated acutely diabetic BB/W rat spleen cells into immunosuppressed diabetes-resistant BB/W control rats and F1 hybrid offspring produced by BB/W X Lewis, BN, Yashida, and NEDH matings. Immune suppression methods that facilitated adoptive transfer of diabetes included neonatal thymectomy, cyclophosphamide, and splenectomy plus rabbit anti-rat lymphocyte serum injections. The successful transfer of BB/W diabetes to otherwise normal (BB/W X inbred)F1 rats and to diabetes-resistant BB/W animals suggests that antigenically normal pancreatic beta cells were destroyed by the injected effector cells. Diabetes-resistant BB/W control rats also evidenced diabetes after the injection of cyclophosphamide alone. The requirement for immunosuppression suggests that an intact immune system protects against adoptive transfer and diabetes in diabetes-resistant BB/W rats.
通过将刀豆蛋白A激活的急性糖尿病BB/W大鼠脾细胞注射到免疫抑制的抗糖尿病BB/W对照大鼠以及由BB/W与Lewis、BN、Yashida和NEDH交配产生的F1杂交后代中,实现糖尿病的过继转移。促进糖尿病过继转移的免疫抑制方法包括新生期胸腺切除、环磷酰胺以及脾切除加兔抗大鼠淋巴细胞血清注射。将BB/W糖尿病成功转移至原本正常的(BB/W×近交系)F1大鼠以及抗糖尿病的BB/W动物,这表明注射的效应细胞破坏了抗原性正常的胰岛β细胞。抗糖尿病的BB/W对照大鼠在单独注射环磷酰胺后也出现了糖尿病。对免疫抑制的需求表明,完整的免疫系统可防止抗糖尿病BB/W大鼠发生糖尿病的过继转移。